MSX2, msh homeobox 2, 4488

N. diseases: 135; N. variants: 7
Disease: Hypodontia ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0020608
Disease: Hypodontia
Hypodontia 		0.010 GeneticVariation disease BEFREE The pairwise lod-scores regarding the intragenic microsatellites in the MSX1 and MSX2 genes at a recombination fraction of 0.0 were -3.1 and -3.0, respectively, thus excluding these genes as causative loci for hypodontia in these families. 7649547 1995